Allele Registry

Canonical Allele Identifier: PA2826236478

Gene: ATP2C1 HGNC NCBI

ClinVar RCV:

RCV000484022

ClinVar Variation:

421924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186114.1:p.Lys589Arg	CA16617827 NM_001199185.2:c.1766A>G