Canonical Allele Identifier: PA2826051780
Gene: KCTD7 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Arg12Leu
CA367695199
NM_001167961.2:c.35G>T