Canonical Allele Identifier: PA916015442
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 827666
ClinVar RCV Id: RCV001027529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Ser47Pro
CA349989865
NM_014585.6:c.139T>C