Canonical Allele Identifier: PA2829884844
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715393
ClinVar RCV Id: RCV002304551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ser2737Thr
CA371307732
NM_017780.4:c.8209T>A