ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA256487
Gene: HRAS
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12603
ClinVar RCV Id:
RCV000013437
RCV000418547
RCV000422263
RCV000430806
RCV000417508
RCV000435619
RCV000423413
RCV000423622
RCV000207503
RCV000440663
RCV000425989
RCV000426130
RCV000428375
RCV000441501
RCV000444092
RCV000433266
RCV000445257
RCV000428172
RCV000433587
RCV000423741
RCV000425511
RCV000623953
RCV000432956
RCV000762848
RCV000435805
RCV000436832
RCV000442448
RCV000445090
RCV001813186
RCV001257536
ClinVar Variation Id:
40430
ClinVar RCV Id:
RCV000157929
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Gly12Ala
CA256486
NM_005343.4:c.35G>C
CA296077
NM_005343.4:c.35_36delinsCT