Canonical Allele Identifier: PA2829600850
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2850846
ClinVar RCV Id: RCV003628532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala66Val
CA378924641
NM_005343.4:c.197C>T