Canonical Allele Identifier: PA2828077155
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 583216
ClinVar RCV Id: RCV000707492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350050.1:p.Ser299Arg
CA4938307
NM_001363121.2:c.897C>A
CA372628259
NM_001363121.2:c.895A>C
CA372628266
NM_001363121.2:c.897C>G