Canonical Allele Identifier: PA2499299277
Gene: KCTD7 HGNC NCBI
ClinVar RCV:
RCV001343197
ClinVar Variation:
1039678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Arg12Leu
CA367695199
NM_153033.5:c.35G>T