Canonical Allele Identifier: PA2828076996
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462730
ClinVar RCV Id: RCV001968613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350050.1:p.Cys126Tyr
CA187657056
NM_001363121.2:c.377G>A