Canonical Allele Identifier: PA2826666378
Gene: KCTD17 HGNC NCBI

Linked Data

ClinVar Variation Id: 191372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269614.2:p.Arg138His
CA199778
NM_001282685.2:c.413G>A