Canonical Allele Identifier: PA2828472467
Gene: SLC29A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164053
ClinVar RCV Id: RCV004458941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001359256.1:p.Gly225Ser
CA3831636
NM_001372327.1:c.673G>A