Canonical Allele Identifier: PA2580380053
Gene: INTU HGNC NCBI

Linked Data

ClinVar Variation Id: 2177687
ClinVar RCV Id: RCV002585668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Pro11Arg
CA3074692
NM_015693.3:c.32C>G