Canonical Allele Identifier: PA1139736001
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 845962
ClinVar RCV Id: RCV001049142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Glu302Gln
CA388694636
NM_001352609.2:c.904G>C