Canonical Allele Identifier: PA2826051833
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432167
ClinVar RCV Id: RCV001959803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.His61Arg
CA4278194
NM_001167961.2:c.182A>G