Canonical Allele Identifier: PA2573283657
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462730
ClinVar RCV Id: RCV001968613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Cys126Tyr
CA187657056
NM_024531.5:c.377G>A