Canonical Allele Identifier: PA2580158862
Gene: PCCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2154348
ClinVar RCV Id: RCV003081740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171485.1:p.Tyr196Cys
CA354739967
NM_001178014.2:c.587A>G