Canonical Allele Identifier: PA2828028919
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470105
ClinVar RCV Id: RCV001190629 RCV003767044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2288_Ser2289del
CA048994
NM_001354906.2:c.6862_6867del