Allele Registry

Canonical Allele Identifier: PA915994224

Gene: PCCB HGNC NCBI

ClinVar Allele:

214551

ClinVar RCV:

RCV000236206

ClinVar Variation:

217894

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171485.1:p.Arg185Trp	CA10575810 NM_001178014.2:c.553C>T