Canonical Allele Identifier: PA2580359106
Gene: SLC40A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2047852
ClinVar RCV Id: RCV002918354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055400.1:p.Ile327Val
CA349987992
NM_014585.6:c.979A>G