Canonical Allele Identifier: PA2827666241
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 3023607
ClinVar RCV Id: RCV003880702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339540.1:p.Val6Ala
CA388694769
NM_001352611.2:c.17T>C