Canonical Allele Identifier: PA103570
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 12018
ClinVar RCV Id: RCV000012798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000523.2:p.Tyr435Cys
CA341178
NM_000532.5:c.1304A>G