Canonical Allele Identifier: PA2741964405
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2733968
ClinVar RCV Id: RCV003499909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Phe2124del
CA2697549948
NM_017780.4:c.6372_6374del