Canonical Allele Identifier: PA1139735967
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 895346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Met216Val
CA2024187
NM_014585.6:c.646A>G