Canonical Allele Identifier: PA2826362299
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 645297
ClinVar RCV Id: RCV000799351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240745.1:p.Leu342Phe
CA4938353
NM_001253816.2:c.1024C>T