Canonical Allele Identifier: PA2828048813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827296
ClinVar RCV Id: RCV001026888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2497Ser
CA16038427
NM_001354904.2:c.7489A>T