Canonical Allele Identifier: PA2828087994
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 806501
ClinVar RCV Id: RCV000994435 RCV002549869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Gly258Ser
CA5543109
NM_001363518.2:c.772G>A