Canonical Allele Identifier: PA1139698745
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 930307
ClinVar RCV Id: RCV001195867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala679Ser
CA371307594
NM_001316690.1:c.2035G>T