Canonical Allele Identifier: PA096973
Gene: INPPL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39479
ClinVar RCV Id: RCV000032675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001558.3:p.Arg401Trp
CA130327
NM_001567.4:c.1201C>T