ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826992638
Gene: INPP5E
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
15436
ClinVar RCV:
RCV000022402
RCV001851510
ClinVar Variation:
397
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305431.1:p.Arg514Trp
CA259595
NM_001318502.2:c.1540C>T