Canonical Allele Identifier: PA101686
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 36926
ClinVar RCV Id: RCV000030608 RCV000519234 RCV000548914 RCV001582502 RCV002513270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Arg184Cys
CA129977
NM_153033.5:c.550C>T