Canonical Allele Identifier: PA2827975947
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692106
ClinVar RCV Id: RCV002255840 RCV003774763 RCV004005551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg1086Leu
CA16028658
NM_001354899.2:c.3257G>T