Canonical Allele Identifier: PA2580413649
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2291871
ClinVar RCV Id: RCV002864800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Asp618Gly
CA371312484
NM_017780.4:c.1853A>G