Canonical Allele Identifier: PA2826131680
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1710761
ClinVar RCV Id: RCV002292048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Ala377Thr
CA7033514
NM_001178004.2:c.1129G>A