Canonical Allele Identifier: PA916027149
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 665396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Thr17Ile
CA4447937
NM_001324401.3:c.50C>T