Canonical Allele Identifier: PA2573275205
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_060814.4:p.Pro277Leu
CA5543062
NM_018344.6:c.830C>T