Allele Registry

Canonical Allele Identifier: PA2825788911

Gene: SLC39A8 HGNC NCBI

ClinVar RCV:

RCV001332456

ClinVar Variation:

1030799

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128619.1:p.Thr308Met	CA3025550 NM_001135147.1:c.923C>T