Allele Registry

Canonical Allele Identifier: PA645448215

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001360520

ClinVar Variation:

246643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Leu1213Phe	CA10584670 NM_001127500.3:c.3637C>T