Allele Registry

Canonical Allele Identifier: PA192402

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000165054

RCV001218524

RCV002498817

RCV003468731

ClinVar Variation:

185606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ala361Ser	CA192400 NM_001127500.3:c.1081G>T