Allele Registry

Canonical Allele Identifier: PA915994216

Gene: PCCB HGNC NCBI

ClinVar RCV:

RCV000032133

ClinVar Variation:

38884

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171485.1:p.Ala173Pro	CA343145 NM_001178014.2:c.517G>C