Canonical Allele Identifier: PA263922
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 56553
ClinVar RCV Id: RCV000049966
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Gly409Glu
CA263921
NM_012434.5:c.1226G>A