Canonical Allele Identifier: PA2579931997
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2416982
ClinVar RCV Id: RCV003111810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ile163Met
CA378921153
NM_001130442.3:c.489C>G