Canonical Allele Identifier: PA645429826
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 333172
ClinVar RCV Id: RCV000396650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Val97Met
CA10611803
NM_014585.6:c.289G>A