Canonical Allele Identifier: PA2826957570
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 241189
ClinVar RCV Id: RCV000229697 RCV000243125 RCV000397991 RCV001002740 RCV001706270 RCV002317769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Gly522Val
CA4759516
NM_001316690.1:c.1565G>T