Canonical Allele Identifier: PA2827975991
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1098Arg
CA008342
NM_001354899.2:c.3294C>G
CA16028729
NM_001354899.2:c.3292A>C
CA16028734
NM_001354899.2:c.3294C>A