Canonical Allele Identifier: PA916071768
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 660897
ClinVar RCV Id: RCV000818197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gly60Ser
CA378924681
NM_176795.5:c.178G>A