Canonical Allele Identifier: PA2829601122
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2128760
ClinVar RCV Id: RCV003057735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Leu159Phe
CA378921178
NM_005343.4:c.477G>T
CA378921179
NM_005343.4:c.477G>C