Canonical Allele Identifier: PA2826051861
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 206012
ClinVar RCV Id: RCV000533139 RCV002426906 RCV001705019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Tyr86His
CA315687
NM_001167961.2:c.256T>C