Canonical Allele Identifier: PA2828088086
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1995947
ClinVar RCV Id: RCV002801682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Thr391Ser
CA377117910
NM_001363518.2:c.1171A>T
CA377117914
NM_001363518.2:c.1172C>G