Canonical Allele Identifier: PA2827966819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1101Arg
CA008342
NM_001354898.2:c.3303C>G
CA16028729
NM_001354898.2:c.3301A>C
CA16028734
NM_001354898.2:c.3303C>A