Canonical Allele Identifier: PA2826343061
Gene: APPL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2231647
ClinVar RCV Id: RCV004093795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001238834.1:p.Arg427Cys
CA6759525
NM_001251905.2:c.1279C>T