Canonical Allele Identifier: PA2825692475
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 935131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Leu168Pro
CA5779216
NM_001130442.3:c.503T>C