Canonical Allele Identifier: PA2828375258
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 476611
ClinVar RCV Id: RCV000537910 RCV000825091 RCV001544835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Asp174Gly
CA9724760
NM_001370086.1:c.521A>G