Canonical Allele Identifier: PA916071599
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240137
ClinVar RCV Id: RCV000232309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Thr2Ala
CA10582926
NM_176795.5:c.4A>G