Allele Registry

Canonical Allele Identifier: PA103526

Gene: PCCB HGNC NCBI

ClinVar Allele:

47483

ClinVar RCV:

RCV000032129

ClinVar Variation:

38880

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Leu519Pro	CA343141 NM_000532.5:c.1556T>C