Canonical Allele Identifier: PA096998
Gene: INPPL1 HGNC NCBI
ClinVar RCV:
RCV000032673
ClinVar Variation:
39477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001558.3:p.Pro659Ser
CA130326
NM_001567.4:c.1975C>T