Canonical Allele Identifier: PA2828012719
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927393
ClinVar RCV Id: RCV001190628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Leu2398Val
CA048920
NM_001354905.2:c.7192C>G