Canonical Allele Identifier: PA2829884832
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2198967
ClinVar RCV Id: RCV002634020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ala2731Thr
CA371307638
NM_017780.4:c.8191G>A