Canonical Allele Identifier: PA916057047
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 800156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu2177Lys
CA4760604
NM_017780.4:c.6529G>A