Canonical Allele Identifier: PA2579930390
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 579709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg164Trp
CA5779220
NM_001130442.3:c.490C>T