Canonical Allele Identifier: PA2579931091
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 850426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg164Pro
CA5779219
NM_001130442.3:c.491G>C