Canonical Allele Identifier: PA2826992638
Gene: INPP5E HGNC NCBI

Linked Data

ClinVar Variation Id: 397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305431.1:p.Arg514Trp
CA259595
NM_001318502.2:c.1540C>T