Canonical Allele Identifier: PA2826891972
Gene: SLC29A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164053
ClinVar RCV Id: RCV004458941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291395.1:p.Gly250Ser
CA3831636
NM_001304466.2:c.748G>A