Canonical Allele Identifier: PA2825692499
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1024818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Pro173Ser
CA378921072
NM_001130442.3:c.517C>T