Canonical Allele Identifier: PA1139725905
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 969276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu2193Lys
CA177354162
NM_017780.4:c.6577G>A