Canonical Allele Identifier: PA645398498
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 267418
ClinVar RCV Id: RCV000258150 RCV001753739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Asn604Lys
CA10602485
NM_017780.4:c.1812C>A
CA371312177
NM_017780.4:c.1812C>G