Canonical Allele Identifier: PA2827977033
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1409Arg
CA038588
NM_001354899.2:c.4226A>G