Canonical Allele Identifier: PA180881
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 177861
ClinVar RCV Id: RCV000154499 RCV000700279
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro140Ser
CA180880
NM_005343.4:c.418C>T