Canonical Allele Identifier: PA2829884932
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1977906
ClinVar RCV Id: RCV002774921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Val2795Met
CA177329414
NM_017780.4:c.8383G>A