Allele Registry

Canonical Allele Identifier: PA2825788836

Gene: SLC39A8 HGNC NCBI

ClinVar RCV:

RCV001680696

RCV003227984

ClinVar Variation:

1271175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128618.1:p.Ala391Thr	CA3025496 NM_001135146.2:c.1171G>A