Canonical Allele Identifier: PA2825644696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366
ClinVar RCV Id: RCV000581808 RCV003538381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Phe2602Tyr
CA16038409
NM_001127511.3:c.7805T>A