Canonical Allele Identifier: PA2827980760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2413101
ClinVar RCV Id: RCV003110116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2543Pro
CA16038081
NM_001354899.2:c.7627T>C