Canonical Allele Identifier: PA2828076784
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Gly341Ser
CA187657684
NM_001363120.2:c.1021G>A