Canonical Allele Identifier: PA916049752
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 642283
ClinVar RCV Id: RCV000795720 RCV002334480 RCV001759504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Val167Ile
CA9724768
NM_033409.4:c.499G>A