Canonical Allele Identifier: PA2573198215
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala684Thr
CA4760967
NM_001316690.1:c.2050G>A