Allele Registry

Canonical Allele Identifier: PA101717

Gene: KCTD7 HGNC NCBI

ClinVar RCV:

RCV000030688

ClinVar Variation:

37011

HGVS (amino-acid)	Matching Registered Transcripts
NP_694578.1:p.Asn273Ile	CA130029 NM_153033.5:c.818A>T