Canonical Allele Identifier: PA2826236071
Gene: ATP2C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5582
ClinVar RCV Id: RCV000005924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186109.1:p.Ala338Thr
CA117622
NM_001199180.2:c.1012G>A