Allele Registry

Canonical Allele Identifier: PA645434569

Gene: PCCB HGNC NCBI

ClinVar Allele:

288925

ClinVar RCV:

RCV000392658

RCV000626699

RCV000859703

RCV003957774

ClinVar Variation:

343477

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Lys474Arg	CA2632188 NM_000532.5:c.1421A>G