Canonical Allele Identifier: PA104613
Gene: INPP5E HGNC NCBI

Linked Data

ClinVar Variation Id: 397
ClinVar RCV Id: RCV000022402 RCV001851510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063945.2:p.Arg515Trp
CA259595
NM_019892.6:c.1543C>T