Canonical Allele Identifier: PA2826131630
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1803092
ClinVar RCV Id: RCV002466762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Ala320Asp
CA388694762
NM_001178004.2:c.959C>A