Canonical Allele Identifier: PA2828374789
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 838277
ClinVar RCV Id: RCV001039792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Gly13Arg
CA9724838
NM_001370085.1:c.37G>A
CA310679445
NM_001370085.1:c.37G>C