Canonical Allele Identifier: PA2825636260
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677427
ClinVar RCV Id: RCV003471648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2674Phe
CA16038755
NM_001127510.3:c.8021C>T