Canonical Allele Identifier: PA2826051852
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372843
ClinVar RCV Id: RCV001908120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Leu77Phe
CA367695607
NM_001167961.2:c.231G>C
CA367695608
NM_001167961.2:c.231G>T