Canonical Allele Identifier: PA2826051841
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 206011
ClinVar RCV Id: RCV000765971 RCV001781555 RCV002314727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Arg65Cys
CA315685
NM_001167961.2:c.193C>T