Canonical Allele Identifier: PA645399498
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 363471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Arg2062Trp
CA10631389
NM_017780.4:c.6184C>T