Allele Registry

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Canonical Allele Identifier: PA2826362962

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_001240782.1:p.Ser143Arg	CA341713739 NM_001253853.3:c.429T>G CA341713741 NM_001253853.3:c.429T>A CA341713748 NM_001253853.3:c.427A>C