Canonical Allele Identifier: PA891856551
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 568628
ClinVar RCV Id: RCV000689049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Trp158Cys
CA349989126
NM_014585.6:c.474G>T
CA349989127
NM_014585.6:c.474G>C