Canonical Allele Identifier: PA2828830248
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9074
ClinVar RCV Id: RCV000009642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366375.1:p.Glu428Asp
CA120092
NM_001379446.1:c.1284G>C
CA384843381
NM_001379446.1:c.1284G>T