Allele Registry

Canonical Allele Identifier: PA2826051891

Gene: KCTD7 HGNC NCBI

ClinVar RCV:

RCV000030689

ClinVar Variation:

37012

HGVS (amino-acid)	Matching Registered Transcripts
NP_001161433.1:p.Asp115Tyr	CA130030 NM_001167961.2:c.343G>T