Canonical Allele Identifier: PA143988
Gene: KCTD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55881
ClinVar RCV Id: RCV000049292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245150.1:p.Ala30Glu
CA143987
NM_001258221.2:c.89C>A