Canonical Allele Identifier: PA2828048508
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_001341833.1:p.Glu2456Gly
CA16038152
NM_001354904.2:c.7367A>G