Canonical Allele Identifier: PA2826051902
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 938692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161433.1:p.Ala124Gly
CA367696222
NM_001167961.2:c.371C>G