Canonical Allele Identifier: PA2580414054
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1696913
ClinVar RCV Id: RCV002267259 RCV003101523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ala1779Val
CA4760343
NM_017780.4:c.5336C>T