Canonical Allele Identifier: PA2828087955
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2548287
ClinVar RCV Id: RCV003262979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ser215Tyr
CA377114420
NM_001363518.2:c.644C>A