Canonical Allele Identifier: PA2826051834
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423573
ClinVar RCV Id: RCV001928933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.His61Asp
CA367695507
NM_001167961.2:c.181C>G