Allele Registry

Canonical Allele Identifier: PA2825620046

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002589570

RCV003871538

ClinVar Variation:

1911045

3017419

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Tyr649His	CA368979474 NM_001127500.3:c.1945T>C CA2740097508 NM_001127500.3:c.1944_1945delinsGC