ClinGen Allele Registry
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Canonical Allele Identifier:
PA103568
Gene: HRAS
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
27642
48900
ClinVar RCV:
RCV000013437
RCV000157929
RCV000207503
RCV000417508
RCV000418547
RCV000422263
RCV000423413
RCV000423622
RCV000423741
RCV000425511
RCV000425989
RCV000426130
RCV000428172
RCV000428375
RCV000430806
RCV000432956
RCV000433266
RCV000433587
RCV000435619
RCV000435805
RCV000436832
RCV000440663
RCV000441501
RCV000442448
RCV000444092
RCV000445090
RCV000445257
RCV000623953
RCV000762848
RCV001257536
RCV001813186
ClinVar Variation:
12603
40430
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001123914.1:p.Gly12Ala
CA256486
NM_001130442.3:c.35G>C
CA296077
NM_001130442.3:c.35_36delinsCT
