Canonical Allele Identifier: PA2741844355
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2734572
ClinVar RCV Id: RCV003513593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Gly182Arg
CA354739659
NM_001178014.2:c.544G>A
CA354739660
NM_001178014.2:c.544G>C