Canonical Allele Identifier: PA257002
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13884
ClinVar RCV Id: RCV000014898 RCV000420939
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Asp1246Asn
CA257000
NM_001127500.3:c.3736G>A