Canonical Allele Identifier: PA2579933426
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1954526
ClinVar RCV Id: RCV002705677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Glu63Asp
CA378924662
NM_001130442.3:c.189G>T
CA378924663
NM_001130442.3:c.189G>C