Canonical Allele Identifier: PA2827665889
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 235532
ClinVar RCV Id: RCV000224898 RCV000675079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339539.1:p.Glu42Asp
CA10581345
NM_001352610.2:c.126G>T
CA388695105
NM_001352610.2:c.126G>C