Allele Registry

Canonical Allele Identifier: PA103517

Gene: PCCB HGNC NCBI

ClinVar Allele:

200029

ClinVar RCV:

RCV000186089

RCV000441240

RCV001083724

RCV003917704

ClinVar Variation:

203883

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Leu17Met	CA312824 NM_000532.5:c.49C>A