Canonical Allele Identifier: PA2826051858
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 469102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Arg84Trp
CA4278209
NM_001167961.2:c.250C>T