Canonical Allele Identifier: PA2830292938
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360043
ClinVar RCV Id: RCV001872400
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689477.3:p.Leu330Pro
CA380315114
NM_152264.5:c.989T>C