Canonical Allele Identifier: PA117629
Gene: ATP2C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5588
ClinVar RCV Id: RCV000005930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001486.1:p.Leu584Pro
CA117628
NM_001001486.2:c.1751T>C