Allele Registry

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Canonical Allele Identifier: PA2828100040

Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1067691

ClinVar RCV Id: RCV001379023

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350535.1:p.Asp1134Glu	CA383582646 NM_001363606.2:c.3402C>G CA383582647 NM_001363606.2:c.3402C>A