Canonical Allele Identifier: PA2829884886
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331252
ClinVar RCV Id: RCV001806597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Gln2765Leu
CA371308142
NM_017780.4:c.8294A>T