Canonical Allele Identifier: PA2741964393
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2850608
ClinVar RCV Id: RCV003604897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu2009Gly
CA371323958
NM_017780.4:c.6026A>G