Canonical Allele Identifier: PA2827982779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1023938
ClinVar RCV Id: RCV003770760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys339Glu
CA16023915
NM_001354900.2:c.1015A>G