Allele Registry

Canonical Allele Identifier: PA2580498756

Gene: KCTD12 HGNC NCBI

ClinVar RCV:

RCV004175934

ClinVar Variation:

2337155

HGVS (amino-acid)	Matching Registered Transcripts
NP_612453.1:p.Gln199Leu	CA388359578 NM_138444.4:c.596A>T