Canonical Allele Identifier: PA315694
Gene: KCTD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 206015
ClinVar RCV Id: RCV000188023 RCV000761541
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694578.1:p.Arg112His
CA315693
NM_153033.5:c.335G>A