Allele Registry

Canonical Allele Identifier: PA916027567

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001360520

ClinVar Variation:

246643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Leu765Phe	CA10584670 NM_001324402.2:c.2293C>T