Canonical Allele Identifier: PA2829884819
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2636862
ClinVar RCV Id: RCV003410823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Arg2727Lys
CA371307571
NM_017780.4:c.8180G>A