Canonical Allele Identifier: PA2826131455
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203875
ClinVar RCV Id: RCV000186079 RCV001193473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Leu146Pro
CA312810
NM_001178004.2:c.437T>C