Canonical Allele Identifier: PA2829884841
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ala2733Thr
CA4760967
NM_017780.4:c.8197G>A