Canonical Allele Identifier: PA2741947598
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606312
ClinVar RCV Id: RCV003369153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.His274Arg
CA349988346
NM_014585.6:c.821A>G