Canonical Allele Identifier: PA2826051836
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781306
ClinVar RCV Id: RCV002412993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Phe62Ser
CA367695516
NM_001167961.2:c.185T>C
CA2580077290
NM_001167961.2:c.185_186delinsCT