Canonical Allele Identifier: PA645399634
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 421081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Asp2197Asn
CA4760613
NM_017780.4:c.6589G>A