Canonical Allele Identifier: PA2826131663
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_001171475.1:p.Glu357Asp
CA10581345
NM_001178004.2:c.1071G>T
CA388695105
NM_001178004.2:c.1071G>C