Canonical Allele Identifier: PA2830508751
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 18095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_958816.1:p.Glu646Asp
CA127797
NM_201413.3:c.1938G>C
CA409806514
NM_201413.3:c.1938G>T