Canonical Allele Identifier: PA2741964368
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2919900
ClinVar RCV Id: RCV003604591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu1789Gly
CA4760344
NM_017780.4:c.5366A>G