Allele Registry

Canonical Allele Identifier: PA915994175

Gene: PCCB HGNC NCBI

ClinVar Allele:

47486

ClinVar RCV:

RCV000032132

ClinVar Variation:

38883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171485.1:p.Gly112Asp	CA343144 NM_001178014.2:c.335G>A