Canonical Allele Identifier: PA915994349
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 225429
ClinVar RCV Id: RCV000490483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Tyr459Cys
CA2632149
NM_001178014.2:c.1376A>G