Canonical Allele Identifier: PA2580527775
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781306
ClinVar RCV Id: RCV002412993
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Phe62Ser
CA367695516
NM_153033.5:c.185T>C
CA2580077290
NM_153033.5:c.185_186delinsCT