Canonical Allele Identifier: PA2573093239
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302957
ClinVar RCV Id: RCV001756456 RCV003603101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Arg2095Gln
CA4760565
NM_017780.4:c.6284G>A