Canonical Allele Identifier: PA891854227
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 589697
ClinVar RCV Id: RCV002317411 RCV003768153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ala2211Val
CA371325990
NM_017780.4:c.6632C>T