Canonical Allele Identifier: PA2828076749
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 583216
ClinVar RCV Id: RCV000707492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ser299Arg
CA4938307
NM_001363120.2:c.897C>A
CA372628259
NM_001363120.2:c.895A>C
CA372628266
NM_001363120.2:c.897C>G