Canonical Allele Identifier: PA094923
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 5418
ClinVar RCV Id: RCV000005751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Gly267Asp
CA117529
NM_014585.6:c.800G>A