Canonical Allele Identifier: PA2573277911
Gene: SLC39A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1486256
ClinVar RCV Id: RCV002003464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071437.3:p.Asp281Asn
CA3025556
NM_022154.5:c.841G>A