Canonical Allele Identifier: PA2829884854
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Leu2744Ser
CA371307839
NM_017780.4:c.8231T>C