Canonical Allele Identifier: PA2828087980
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1358429
ClinVar RCV Id: RCV001864082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Pro246Ser
CA377115219
NM_001363518.2:c.736C>T