Canonical Allele Identifier: PA2828087948
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 130346
ClinVar RCV Id: RCV000118384 RCV000312318 RCV001572870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Leu203Pro
CA155250
NM_001363518.2:c.608T>C