Canonical Allele Identifier: PA658817022
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 498284
ClinVar RCV Id: RCV000595997 RCV001854018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Lys1759Gln
CA4760315
NM_017780.4:c.5275A>C