Canonical Allele Identifier: PA315697
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 206017
ClinVar RCV Id: RCV000188025 RCV001852471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Trp235Ser
CA315696
NM_153033.5:c.704G>C