Allele Registry

Canonical Allele Identifier: PA2828796139

Gene: ATP2C1 HGNC NCBI

ClinVar RCV:

RCV000484022

ClinVar Variation:

421924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365616.1:p.Lys589Arg	CA16617827 NM_001378687.1:c.1766A>G