Canonical Allele Identifier: PA2579931737
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 177861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Pro140Ser
CA180880
NM_001130442.3:c.418C>T