Canonical Allele Identifier: PA2579930696
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2817156
ClinVar RCV Id: RCV003627913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asp154Tyr
CA378921228
NM_001130442.3:c.460G>T