Canonical Allele Identifier: PA166141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141690
ClinVar RCV Id: RCV000130304 RCV000765791 RCV001549810 RCV002469020 RCV003998055 RCV003430706 RCV003764867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg2741His
CA014525
NM_001127511.3:c.8222G>A