Canonical Allele Identifier: PA916076130
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 645041
ClinVar RCV Id: RCV000799056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Pro134Leu
CA372627081
NM_024531.5:c.401C>T