Canonical Allele Identifier: PA101733
Gene: KCTD7 HGNC NCBI
ClinVar RCV:
RCV000030690
ClinVar Variation:
37013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Leu108Met
CA130032
NM_153033.5:c.322C>A