Canonical Allele Identifier: PA2499290325
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047525
ClinVar RCV Id: RCV001352249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Ser49Pro
CA372626168
NM_024531.5:c.145T>C