Canonical Allele Identifier: PA2826236449
Gene: ATP2C1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186114.1:p.Ala304Thr
CA117622
NM_001199185.2:c.910G>A