Canonical Allele Identifier: PA2825018760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1385987
ClinVar RCV Id: RCV003534768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu1111Gln
CA16028636
NM_000038.6:c.3331G>C