Canonical Allele Identifier: PA2829884810
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 910664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ser2723Asn
CA4760958
NM_017780.4:c.8168G>A