Canonical Allele Identifier: PA110925
Gene: ATP2C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5588
ClinVar RCV Id: RCV000005930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186108.1:p.Leu584Pro
CA117628
NM_001199179.3:c.1751T>C