Canonical Allele Identifier: PA103991
Gene: KCTD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55881
ClinVar RCV Id: RCV000049292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129677.1:p.Ala30Glu
CA143987
NM_001136205.2:c.89C>A