Canonical Allele Identifier: PA2830041042
Gene: KCTD17 HGNC NCBI

Linked Data

ClinVar Variation Id: 191372
ClinVar RCV Id: RCV000171554 RCV001092006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078957.3:p.Arg138His
CA199778
NM_024681.4:c.413G>A