Canonical Allele Identifier: PA2580401206
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169550
ClinVar RCV Id: RCV003084885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Pro391His
CA5543135
NM_018344.6:c.1172C>A