Canonical Allele Identifier: PA2827970665
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567068
ClinVar RCV Id: RCV003311060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly2268Ala
CA16036342
NM_001354898.2:c.6803G>C