Canonical Allele Identifier: PA2825187410
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 1483561
ClinVar RCV Id: RCV002003198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Leu158Val
CA354739623
NM_000532.5:c.472C>G