Canonical Allele Identifier: PA2829884818
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2880622
ClinVar RCV Id: RCV003602790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ala2726Ser
CA371307552
NM_017780.4:c.8176G>T