Canonical Allele Identifier: PA2826977557
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 946957
ClinVar RCV Id: RCV001217922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Met103Leu
CA378920954
NM_001318054.2:c.307A>C
CA378920956
NM_001318054.2:c.307A>T