Canonical Allele Identifier: PA2827980754
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_001341828.1:p.Ser2543_Ser2544del
CA048994
NM_001354899.2:c.7627_7632del