Canonical Allele Identifier: PA2825210682
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3162806
ClinVar RCV Id: RCV004456205
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000608.1:p.Ala371Val
CA384843755
NM_000617.3:c.1112C>T