Canonical Allele Identifier: PA1139677743
Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 897923
ClinVar RCV Id: RCV001141462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000475.1:p.Lys725Asn
CA409805496
NM_000484.4:c.2175G>T
CA409805497
NM_000484.4:c.2175G>C