Canonical Allele Identifier: PA103583
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 225429
ClinVar RCV Id: RCV000490483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Tyr439Cys
CA2632149
NM_000532.5:c.1316A>G