Canonical Allele Identifier: PA2828909433
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2435976
ClinVar RCV Id: RCV003136726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369558.1:p.Asn246Ser
CA3890388
NM_001382629.1:c.737A>G