Canonical Allele Identifier: PA2825368327
Gene: SLC29A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 503838
ClinVar RCV Id: RCV000599370
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035751.1:p.Ala39_Gln41dup
CA658796899
NM_001040661.3:c.116_124dup