Canonical Allele Identifier: PA916021793
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 666812
ClinVar RCV Id: RCV000825312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Asp739His
CA371308681
NM_001316690.1:c.2215G>C