Allele Registry

Canonical Allele Identifier: PA2826051883

Gene: KCTD7 HGNC NCBI

ClinVar RCV:

RCV000030690

ClinVar Variation:

37013

HGVS (amino-acid)	Matching Registered Transcripts
NP_001161433.1:p.Leu108Met	CA130032 NM_001167961.2:c.322C>A