Canonical Allele Identifier: PA2579931281
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2146977
ClinVar RCV Id: RCV003076952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Thr158Arg
CA378921185
NM_001130442.3:c.473C>G