Canonical Allele Identifier: PA2573275226
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379589
ClinVar RCV Id: RCV001914889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ile301Asn
CA377114578
NM_018344.6:c.902T>A