Canonical Allele Identifier: PA2826977559
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1038544
ClinVar RCV Id: RCV001341872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Met103Thr
CA378920950
NM_001318054.2:c.308T>C