Canonical Allele Identifier: PA2828049098
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946346
ClinVar RCV Id: RCV003650722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2544Thr
CA16038730
NM_001354904.2:c.7631G>C