Canonical Allele Identifier: PA915994346
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 12018
ClinVar RCV Id: RCV000012798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Tyr455Cys
CA341178
NM_001178014.2:c.1364A>G