Canonical Allele Identifier: PA915983894
Gene: KCTD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55888
ClinVar RCV Id: RCV000049299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245151.1:p.Gly70Asp
CA144001
NM_001258222.3:c.209G>A