Canonical Allele Identifier: PA645495500
Gene: SLC6A17 HGNC NCBI

Linked Data

ClinVar Variation Id: 436763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010898.1:p.Arg275Gln
CA998003
NM_001010898.4:c.824G>A