Canonical Allele Identifier: PA2828002372
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482319
ClinVar RCV Id: RCV000570780 RCV001546318 RCV003105965 RCV004000967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1433Val
CA16031338
NM_001354902.2:c.4297A>G