Allele Registry

Canonical Allele Identifier: PA2825622265

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002012246

ClinVar Variation:

1448825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Tyr1248Asp	CA368991595 NM_001127500.3:c.3742T>G