Canonical Allele Identifier: PA2827989879
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827236
ClinVar RCV Id: RCV001026779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu2541Gly
CA16038152
NM_001354900.2:c.7622A>G