Canonical Allele Identifier: PA243788
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 196709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Gly2103Asp
CA243786
NM_017780.4:c.6308G>A