Allele Registry

Canonical Allele Identifier: PA658803538

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628755

RCV001010899

RCV001312217

ClinVar Variation:

524876

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Glu436Lys	CA368972893 NM_001127500.3:c.1306G>A