Canonical Allele Identifier: PA2825692573
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 940755
ClinVar RCV Id: RCV001210405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ser189Phe
CA378920852
NM_001130442.3:c.566C>T