Canonical Allele Identifier: PA658811741
Gene: SLC29A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 503838
ClinVar RCV Id: RCV000599370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694979.2:p.Ala39_Gln41dup
CA658796899
NM_153247.4:c.116_124dup