Canonical Allele Identifier: PA2741858774
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2636862
ClinVar RCV Id: RCV003410823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Arg678Lys
CA371307571
NM_001316690.1:c.2033G>A