Allele Registry

Canonical Allele Identifier: PA2826400339

Gene: SLC39A2 HGNC NCBI

ClinVar RCV:

RCV001645979

ClinVar Variation:

1243818

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243517.1:p.Leu43Arg	CA7084761 NM_001256588.2:c.128T>G