Canonical Allele Identifier: PA245488
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 197381
ClinVar RCV Id: RCV000178394 RCV001852214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Gly265Arg
CA245487
NM_153033.5:c.793G>A
CA367697602
NM_153033.5:c.793G>C