Canonical Allele Identifier: PA2826051849
Gene: KCTD7 HGNC NCBI
ClinVar RCV:
RCV002681504
ClinVar Variation:
1950810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Thr75Ile
CA367695594
NM_001167961.2:c.224C>T