Canonical Allele Identifier: PA2580197661
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1902877
ClinVar RCV Id: RCV002583261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Gly725Ser
CA371308340
NM_001316690.1:c.2173G>A