Canonical Allele Identifier: PA2741955256
Gene: INTU HGNC NCBI

Linked Data

ClinVar Variation Id: 2907596
ClinVar RCV Id: RCV003727217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Glu25del
CA3074698
NM_015693.3:c.75_77del