Canonical Allele Identifier: PA2828076520
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047525
ClinVar RCV Id: RCV001352249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ser49Pro
CA372626168
NM_001363120.2:c.145T>C