Canonical Allele Identifier: PA2828910886
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2563375
ClinVar RCV Id: RCV003301536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369564.1:p.Ala432Val
CA364720026
NM_001382635.1:c.1295C>T