Allele Registry

Canonical Allele Identifier: PA2499249455

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001553682

ClinVar Variation:

1192249

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Val790Leu	CA368991469 NM_001324402.2:c.2368G>C