Canonical Allele Identifier: PA915994323
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 217891
ClinVar RCV Id: RCV000235547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Glu424Lys
CA2632093
NM_001178014.2:c.1270G>A