Canonical Allele Identifier: PA103378
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 30949
ClinVar RCV Id: RCV000023939 RCV000493511 RCV003398566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Arg363Trp
CA129562
NM_018344.6:c.1087C>T