Canonical Allele Identifier: PA2826343010
Gene: APPL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128088
ClinVar RCV Id: RCV004419991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001238833.1:p.Phe480Leu
CA386376009
NM_001251904.2:c.1440T>G
CA386376011
NM_001251904.2:c.1440T>A
CA386376023
NM_001251904.2:c.1438T>C