Canonical Allele Identifier: PA2826131711
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1490406
ClinVar RCV Id: RCV001983721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Arg399Leu
CA388695374
NM_001178004.2:c.1196G>T