Canonical Allele Identifier: PA2573265132
Gene: INTU HGNC NCBI

Linked Data

ClinVar Variation Id: 1393254
ClinVar RCV Id: RCV001882363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Arg89Ser
CA358133173
NM_015693.3:c.267G>C
CA358133174
NM_015693.3:c.267G>T