Canonical Allele Identifier: PA209402
Gene: INPP5E HGNC NCBI

Linked Data

ClinVar Variation Id: 211185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063945.2:p.Arg292His
CA209401
NM_019892.6:c.875G>A