Allele Registry

Canonical Allele Identifier: PA915994139

Gene: PCCB HGNC NCBI

ClinVar Allele:

200029

ClinVar RCV:

RCV000186089

RCV000441240

RCV001083724

RCV003917704

ClinVar Variation:

203883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171485.1:p.Leu17Met	CA312824 NM_001178014.2:c.49C>A