Canonical Allele Identifier: PA658803598
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 446117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Tyr1252Cys
CA368991650
NM_001127500.3:c.3755A>G