Allele Registry

Canonical Allele Identifier: PA212647

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000185580

RCV000202585

ClinVar Variation:

183686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Phe859Val	CA212644 NM_001127500.3:c.2575T>G