Canonical Allele Identifier: PA2579931576
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gln61Lys
CA122547
NM_001130442.3:c.181C>A