Canonical Allele Identifier: PA2741964256
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2816109
ClinVar RCV Id: RCV003604252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Pro588Ser
CA371311792
NM_017780.4:c.1762C>T