Allele Registry

Canonical Allele Identifier: PA114708

Gene: SLC30A8 HGNC NCBI

ClinVar RCV:

RCV000001055

RCV003974786

ClinVar Variation:

1000

HGVS (amino-acid)	Matching Registered Transcripts
NP_776250.2:p.Arg325Trp	CA114706 NM_173851.3:c.973C>T