Allele Registry

Canonical Allele Identifier: PA3057530054

Gene: APP HGNC NCBI

ClinVar RCV:

RCV005168170

ClinVar Variation:

3690355

HGVS (amino-acid)	Matching Registered Transcripts
NP_958817.1:p.Ala638Glu	CA409805566 NM_201414.3:c.1913C>A