Canonical Allele Identifier: PA2828036467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127283
ClinVar RCV Id: RCV000115076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro898Ser
CA008017
NM_001354904.2:c.2692C>T