Canonical Allele Identifier: PA2579931432
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1713326
ClinVar RCV Id: RCV002302904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Glu162Gln
CA378921166
NM_001130442.3:c.484G>C