Allele Registry

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Canonical Allele Identifier: PA2826362735

Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2623900

ClinVar RCV Id: RCV003377325

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001240781.1:p.Ser242Arg	CA341713739 NM_001253852.3:c.726T>G CA341713741 NM_001253852.3:c.726T>A CA341713748 NM_001253852.3:c.724A>C