Canonical Allele Identifier: PA2826957942
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1805567
ClinVar RCV Id: RCV002471985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Pro516Ser
CA371303399
NM_001316690.1:c.1546C>T