Canonical Allele Identifier: PA658817111
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 529123
ClinVar RCV Id: RCV000634423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Pro2776Ser
CA4760989
NM_017780.4:c.8326C>T