Canonical Allele Identifier: PA916035567
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38865
ClinVar RCV Id: RCV000032108 RCV000127322 RCV002262596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Val551Phe
CA292687
NM_001352609.2:c.1651G>T