Canonical Allele Identifier: PA2573070074
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1306150
ClinVar RCV Id: RCV001767103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Leu696Val
CA371307848
NM_001316690.1:c.2086C>G