Allele Registry

Canonical Allele Identifier: PA645448131

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000476062

RCV001018130

RCV001312218

RCV001755706

RCV001788226

ClinVar Variation:

411918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Pro1009Ser	CA4448619 NM_001127500.3:c.3025C>T