Canonical Allele Identifier: PA2580380101
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV002631472
ClinVar Variation:
1931255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Gly223Ser
CA105646654
NM_015693.3:c.667G>A