Canonical Allele Identifier: PA2826052021
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 37011
ClinVar RCV Id: RCV000030688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Asn273Ile
CA130029
NM_001167961.2:c.818A>T