Canonical Allele Identifier: PA916021786
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 648106
ClinVar RCV Id: RCV000802758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Lys673Glu
CA371307448
NM_001316690.1:c.2017A>G