Canonical Allele Identifier: PA2826361674
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520932
ClinVar RCV Id: RCV002031012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240744.1:p.Lys75Arg
CA372626506
NM_001253815.2:c.224A>G