Canonical Allele Identifier: PA2580414183
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718519
ClinVar RCV Id: RCV002296657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Lys2201Asn
CA371325888
NM_017780.4:c.6603G>C
CA371325890
NM_017780.4:c.6603G>T