Allele Registry

Canonical Allele Identifier: PA332691

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000123130

RCV000567143

RCV001527318

RCV003467091

ClinVar Variation:

135974

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ser22Ile	CA332689 NM_001127500.3:c.65G>T