Canonical Allele Identifier: PA1139726291
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 855829
ClinVar RCV Id: RCV001061170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Phe2545Ser
CA371304213
NM_017780.4:c.7634T>C