Canonical Allele Identifier: PA2825817992
Gene: APP HGNC NCBI
ClinVar RCV:
RCV003223103
ClinVar Variation:
2498894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129601.1:p.Ile585Phe
CA409805555
NM_001136129.3:c.1753A>T