Canonical Allele Identifier: PA346972
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210013
ClinVar RCV Id: RCV000191958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Gly54Arg
CA346971
NM_033409.4:c.160G>A
CA407964415
NM_033409.4:c.160G>C