Canonical Allele Identifier: PA2826131458
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2197660
ClinVar RCV Id: RCV002640217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Lys150Arg
CA7033229
NM_001178004.2:c.449A>G