Canonical Allele Identifier: PA2825139178
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_000273.2:p.Arg399Leu
CA388695374
NM_000282.4:c.1196G>T