Canonical Allele Identifier: PA916041179
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371858
ClinVar RCV Id: RCV000409487 RCV003743703 RCV003343801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2284_Ser2288del
CA16042098
NM_001354896.2:c.6850_6864del