Canonical Allele Identifier: PA2828783014
Gene: ATP2C1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365441.1:p.Ala304Thr
CA117622
NM_001378512.1:c.910G>A