Allele Registry

Canonical Allele Identifier: PA103389

Gene: PCCB HGNC NCBI

ClinVar Allele:

27050

ClinVar RCV:

RCV000012791

ClinVar Variation:

12011

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Arg410Trp	CA343136 NM_000532.5:c.1228C>T