Canonical Allele Identifier: PA2825021358
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745359
ClinVar RCV Id: RCV002336002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln1701Pro
CA16032485
NM_000038.6:c.5102A>C