Canonical Allele Identifier: PA2579931656
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala59Thr
CA176353
NM_001130442.3:c.175G>A