Canonical Allele Identifier: PA916040228
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469962
ClinVar RCV Id: RCV000708640 RCV001155476 RCV002526273 RCV003328596 RCV003999394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1466Ile
CA16030848
NM_001354896.2:c.4397C>T