Allele Registry

Canonical Allele Identifier: PA915994349

Gene: PCCB HGNC NCBI

ClinVar RCV:

RCV000490483

ClinVar Variation:

225429

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171485.1:p.Tyr459Cys	CA2632149 NM_001178014.2:c.1376A>G