Canonical Allele Identifier: PA2741955272
Gene: INTU HGNC NCBI
ClinVar RCV:
RCV003681743
ClinVar Variation:
2803880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056508.2:p.Thr171Ala
CA3074807
NM_015693.3:c.511A>G