Canonical Allele Identifier: PA891850524
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 580753
ClinVar RCV Id: RCV000704391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ile163Phe
CA378921157
NM_005343.4:c.487A>T