Canonical Allele Identifier: PA2828032200
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1765531
ClinVar RCV Id: RCV002376454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro276Leu
CA16023291
NM_001354904.2:c.827C>T