Allele Registry

Canonical Allele Identifier: PA2825143213

Gene: SLC12A3 HGNC NCBI

ClinVar Allele:

390646

ClinVar RCV:

RCV000454555

ClinVar Variation:

403666

HGVS (amino-acid)	Matching Registered Transcripts
NP_000330.3:p.Asn426Tyr	CA16609823 NM_000339.3:c.1276A>T