Canonical Allele Identifier: PA2499283778
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1028057
ClinVar RCV Id: RCV001329005 RCV002546298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Tyr1616Cys
CA177350049
NM_017780.4:c.4847A>G