Canonical Allele Identifier: PA2499283790
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034863
ClinVar RCV Id: RCV001337647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Pro2029Thr
CA371324111
NM_017780.4:c.6085C>A