Canonical Allele Identifier: PA2826131451
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203880
ClinVar RCV Id: RCV000186085 RCV000414788 RCV003984829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Gly142Asp
CA312819
NM_001178004.2:c.425G>A