Canonical Allele Identifier: PA2580197651
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715393
ClinVar RCV Id: RCV002304551
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ser688Thr
CA371307732
NM_001316690.1:c.2062T>A