Canonical Allele Identifier: PA346976
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210015
ClinVar RCV Id: RCV000191960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Glu71Lys
CA346975
NM_033409.4:c.211G>A