Canonical Allele Identifier: PA2580197653
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Asn693His
CA4760970
NM_001316690.1:c.2077A>C