Canonical Allele Identifier: PA2741955258
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV003833346
ClinVar Variation:
2973772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Ala44Val
CA3074712
NM_015693.3:c.131C>T