Allele Registry

Canonical Allele Identifier: PA103338

Gene: PCCB HGNC NCBI

ClinVar Allele:

47487

ClinVar RCV:

RCV000032133

ClinVar Variation:

38884

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Ala153Pro	CA343145 NM_000532.5:c.457G>C