Canonical Allele Identifier: PA658669408
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 454211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ala800Thr
CA368982475
NM_001127500.3:c.2398G>A