Canonical Allele Identifier: PA2580532822
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1954526
ClinVar RCV Id: RCV002705677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Glu63Asp
CA378924662
NM_176795.5:c.189G>T
CA378924663
NM_176795.5:c.189G>C