Allele Registry

Canonical Allele Identifier: PA2825619181

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001324775

ClinVar Variation:

1024574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ser441Cys	CA368972928 NM_001127500.3:c.1322C>G