Canonical Allele Identifier: PA2741964412
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2894902
ClinVar RCV Id: RCV003603527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ile2162Ser
CA371325420
NM_017780.4:c.6485T>G