Canonical Allele Identifier: PA2829884848
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136122
ClinVar RCV Id: RCV003037014 RCV003603130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Asn2742His
CA4760970
NM_017780.4:c.8224A>C