Canonical Allele Identifier: PA2573270450
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439188
ClinVar RCV Id: RCV001958054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu2012Val
CA371323979
NM_017780.4:c.6035A>T