Canonical Allele Identifier: PA2742019202
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2850846
ClinVar RCV Id: RCV003628532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ala66Val
CA378924641
NM_176795.5:c.197C>T