Canonical Allele Identifier: PA1139765491
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 911917
ClinVar RCV Id: RCV001164719 RCV003284009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.His61Tyr
CA4278193
NM_153033.5:c.181C>T