Canonical Allele Identifier: PA2828088025
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025167
ClinVar RCV Id: RCV001325449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Val305Leu
CA5543130
NM_001363518.2:c.913G>C
CA377116926
NM_001363518.2:c.913G>T