Canonical Allele Identifier: PA916042152
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470045
ClinVar RCV Id: RCV000583903 RCV000602624 RCV003999413 RCV003742764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg223Gln
CA16022735
NM_001354902.2:c.668G>A