Allele Registry

Canonical Allele Identifier: PA645434405

Gene: PCCB HGNC NCBI

ClinVar RCV:

RCV000325301

RCV001706552

RCV003950206

ClinVar Variation:

343467

HGVS (amino-acid)	Matching Registered Transcripts
NP_000523.2:p.Pro199Ser	CA2631791 NM_000532.5:c.595C>T