Allele Registry

Canonical Allele Identifier: PA2580542328

Gene: SLC9C2 HGNC NCBI

ClinVar RCV:

RCV004095422

ClinVar Variation:

2230262

HGVS (amino-acid)	Matching Registered Transcripts
NP_848622.2:p.Lys573Glu	CA343759119 NM_178527.4:c.1717A>G