Canonical Allele Identifier: PA2828076588
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1061238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ala124Ser
CA4938175
NM_001363120.2:c.370G>T