Allele Registry

Canonical Allele Identifier: PA2826343061

Gene: APPL2 HGNC NCBI

ClinVar Allele:

2223686

ClinVar RCV:

RCV004093795

ClinVar Variation:

2231647

HGVS (amino-acid)	Matching Registered Transcripts
NP_001238834.1:p.Arg427Cys	CA6759525 NM_001251905.2:c.1279C>T