Canonical Allele Identifier: PA2741955271
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV003816975
ClinVar Variation:
2958752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Lys168Arg
CA3074805
NM_015693.3:c.503A>G