Canonical Allele Identifier: PA2826957447
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 501221
ClinVar RCV Id: RCV000727319 RCV001854082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ile304Thr
CA4759404
NM_001316690.1:c.911T>C