Canonical Allele Identifier: PA2499247841
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala665Val
CA4760955
NM_001316690.1:c.1994C>T