Canonical Allele Identifier: PA916022178
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 580753
ClinVar RCV Id: RCV000704391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ile84Phe
CA378921157
NM_001318054.2:c.250A>T