Canonical Allele Identifier: PA1139677743
Gene: APP HGNC NCBI

Linked Data


Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000475.1:p.Lys725Asn
NM_000484.4:c.2175G>C

NM_000484.4:c.2175G>T