Canonical Allele Identifier: PA658677638
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV000515931
ClinVar Variation:
446689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Arg543His
CA3075153
NM_015693.3:c.1628G>A