Canonical Allele Identifier: PA101692
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 469102
ClinVar RCV Id: RCV000554978 RCV002282222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Arg84Trp
CA4278209
NM_153033.5:c.250C>T