Canonical Allele Identifier: PA2827666612
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1991548
ClinVar RCV Id: RCV002790703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Leu107Val
CA388695857
NM_001352612.2:c.319C>G