Canonical Allele Identifier: PA645495498
Gene: SLC6A17 HGNC NCBI

Linked Data

ClinVar Variation Id: 187769
ClinVar RCV Id: RCV000167526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010898.1:p.Gly162Arg
CA997928
NM_001010898.4:c.484G>A
CA341569939
NM_001010898.4:c.484G>C