Canonical Allele Identifier: PA2825018226
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2122352
ClinVar RCV Id: RCV003744979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu1029Arg
CA16028093
NM_000038.6:c.3086T>G