Canonical Allele Identifier: PA645399793
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 379211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Phe2750Leu
CA4760972
NM_017780.4:c.8250T>G
CA371307922
NM_017780.4:c.8248T>C
CA371307931
NM_017780.4:c.8250T>A