Canonical Allele Identifier: PA916071811
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40438
ClinVar RCV Id: RCV000207497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ser89Cys
CA351483
NM_176795.5:c.266C>G