Canonical Allele Identifier: PA2573093279
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311800
ClinVar RCV Id: RCV001752783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Lys2186Ile
CA4760608
NM_017780.4:c.6557A>T