Allele Registry

Canonical Allele Identifier: PA658804607

Gene: PCCB HGNC NCBI

ClinVar RCV:

RCV000634872

RCV001193212

ClinVar Variation:

529437

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Gly162Trp	CA2631758 NM_000532.5:c.484G>T