Canonical Allele Identifier: PA2741965653
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2776179
ClinVar RCV Id: RCV003645967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Phe317del
CA2609558661
NM_018344.6:c.949_951del