Canonical Allele Identifier: PA2826957788
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344751
ClinVar RCV Id: RCV001849752 RCV002545278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ser244Arg
CA4759366
NM_001316690.1:c.732C>G
CA371299054
NM_001316690.1:c.730A>C
CA371299068
NM_001316690.1:c.732C>A