Canonical Allele Identifier: PA915994222
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 529437
ClinVar RCV Id: RCV000634872 RCV001193212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Gly182Trp
CA2631758
NM_001178014.2:c.544G>T