Canonical Allele Identifier: PA2827609725
Gene: KCTD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55888
ClinVar RCV Id: RCV000049299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338372.1:p.Gly62Asp
CA144001
NM_001351443.1:c.185G>A