Canonical Allele Identifier: PA2830359795
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 409951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Leu133His
CA5779320
NM_176795.5:c.398T>A