Canonical Allele Identifier: PA2828374831
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210015
ClinVar RCV Id: RCV000191960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Glu71Lys
CA346975
NM_001370085.1:c.211G>A