Allele Registry

Canonical Allele Identifier: PA645448225

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000437499

ClinVar Variation:

376728

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Asp1246His	CA16603136 NM_001127500.3:c.3736G>C