Canonical Allele Identifier: PA658677633
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV000515956
ClinVar Variation:
446695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Arg430Cys
CA358147148
NM_015693.3:c.1288C>T