Canonical Allele Identifier: PA2829887432
Gene: APPL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128088
ClinVar RCV Id: RCV004419991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060641.2:p.Phe474Leu
CA386376009
NM_018171.5:c.1422T>G
CA386376011
NM_018171.5:c.1422T>A
CA386376023
NM_018171.5:c.1420T>C