Canonical Allele Identifier: PA2825210720
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309304
ClinVar RCV Id: RCV000390498
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000608.1:p.Ala555Thr
CA6566428
NM_000617.3:c.1663G>A