Canonical Allele Identifier: PA645375487
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 300367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Phe316Val
CA5543092
NM_018344.6:c.946T>G