Allele Registry

Canonical Allele Identifier: PA103583

Gene: PCCB HGNC NCBI

ClinVar Allele:

227253

ClinVar RCV:

RCV000490483

ClinVar Variation:

225429

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Tyr439Cys	CA2632149 NM_000532.5:c.1316A>G