Canonical Allele Identifier: PA2828910711
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2147560
ClinVar RCV Id: RCV003060957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369564.1:p.Asn77Asp
CA364718873
NM_001382635.1:c.229A>G