Canonical Allele Identifier: PA916015513
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 698027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Pro443Leu
CA2024082
NM_014585.6:c.1328C>T