Canonical Allele Identifier: PA916071809
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 580944
ClinVar RCV Id: RCV000704627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Cys80Ser
CA378924541
NM_176795.5:c.239G>C
CA378924550
NM_176795.5:c.238T>A