Canonical Allele Identifier: PA2825692562
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1713318
ClinVar RCV Id: RCV002304250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Val187Met
CA378920877
NM_001130442.3:c.559G>A