Canonical Allele Identifier: PA2825636172
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_001120982.1:p.Thr2623Ser
CA16038427
NM_001127510.3:c.7867A>T