Canonical Allele Identifier: PA2826343063
Gene: APPL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128088
ClinVar RCV Id: RCV004419991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001238834.1:p.Phe431Leu
CA386376009
NM_001251905.2:c.1293T>G
CA386376011
NM_001251905.2:c.1293T>A
CA386376023
NM_001251905.2:c.1291T>C