Canonical Allele Identifier: PA2741964401
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2571693
ClinVar RCV Id: RCV003313402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Gly2108Glu
CA371324790
NM_017780.4:c.6323G>A