Allele Registry

Canonical Allele Identifier: PA103380

Gene: PCCB HGNC NCBI

ClinVar Allele:

214551

ClinVar RCV:

RCV000236206

ClinVar Variation:

217894

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Arg165Trp	CA10575810 NM_000532.5:c.493C>T