Allele Registry

Canonical Allele Identifier: PA2825788967

Gene: SLC39A8 HGNC NCBI

ClinVar RCV:

RCV001332456

ClinVar Variation:

1030799

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128620.1:p.Thr241Met	CA3025550 NM_001135148.2:c.722C>T