Canonical Allele Identifier: PA916035529
Gene: PCCA HGNC NCBI
ClinVar Allele:
47473
ClinVar RCV:
RCV000032111
ClinVar Variation:
38868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Ile164Thr
CA343124
NM_001352609.2:c.491T>C