Canonical Allele Identifier: PA2741955261
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV003729682
ClinVar Variation:
2908257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Ser77Gly
CA358133093
NM_015693.3:c.229A>G