Canonical Allele Identifier: PA2828076780
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 962246
ClinVar RCV Id: RCV001236064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ala337Val
CA372628799
NM_001363120.2:c.1010C>T