Canonical Allele Identifier: PA2826051823
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1441182
ClinVar RCV Id: RCV001967853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Glu51Asp
CA367695450
NM_001167961.2:c.153G>C
CA367695451
NM_001167961.2:c.153G>T