Canonical Allele Identifier: PA2741964414
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2506851
ClinVar RCV Id: RCV003237220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ala2209Val
CA371325981
NM_017780.4:c.6626C>T