ClinGen Allele Registry
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Canonical Allele Identifier:
PA122556
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1664450272
Score
0.0209793543
Score
-0.080607077
Score
0
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013446
RCV000029210
RCV000038460
RCV000149830
RCV000212496
RCV000429375
RCV001255681
RCV001375956
RCV001678586
RCV001813189
ClinVar Variation:
12612
180854
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Gly12Asp
CA122555
NM_005343.4:c.35G>A
CA296072
NM_005343.4:c.35_36delinsAT