Canonical Allele Identifier: PA2573183028
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_001121697.2:p.Leu337Pro
CA380315114
NM_001128225.3:c.1010T>C