Canonical Allele Identifier: PA916041605
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_001341825.1:p.Thr2641Ser
CA16038427
NM_001354896.2:c.7921A>T