Canonical Allele Identifier: PA2828087944
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432623
ClinVar RCV Id: RCV001943996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Pro199Leu
CA5543062
NM_001363518.2:c.596C>T