Canonical Allele Identifier: PA292688
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_000273.2:p.Val551Phe
CA292687
NM_000282.4:c.1651G>T