Canonical Allele Identifier: PA2828375211
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Ala107Val
CA407964082
NM_001370086.1:c.320C>T