Canonical Allele Identifier: PA2580401240
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1995947
ClinVar RCV Id: RCV002801682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Thr469Ser
CA377117910
NM_018344.6:c.1405A>T
CA377117914
NM_018344.6:c.1406C>G