Canonical Allele Identifier: PA658816984
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 529125
ClinVar RCV Id: RCV000634426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ile1010Met
CA371309369
NM_017780.4:c.3030A>G