Canonical Allele Identifier: PA2828783198
Gene: ATP2C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5588
ClinVar RCV Id: RCV000005930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365443.1:p.Leu568Pro
CA117628
NM_001378514.1:c.1703T>C