Canonical Allele Identifier: PA2825024695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009233
ClinVar RCV Id: RCV003770591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu2558Phe
CA16037997
NM_000038.6:c.7672C>T