Canonical Allele Identifier: PA2580197647
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2073337
ClinVar RCV Id: RCV002944032 RCV003250664 RCV003906416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala677Thr
CA4760960
NM_001316690.1:c.2029G>A