Canonical Allele Identifier: PA2580414342
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2146612
ClinVar RCV Id: RCV003067221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Arg2568Gln
CA177325600
NM_017780.4:c.7703G>A