Canonical Allele Identifier: PA1139698743
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 910664
ClinVar RCV Id: RCV001162607 RCV001303651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ser674Asn
CA4760958
NM_001316690.1:c.2021G>A