Canonical Allele Identifier: PA2828019651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser843Arg
CA008342
NM_001354906.2:c.2529C>G
CA16028729
NM_001354906.2:c.2527A>C
CA16028734
NM_001354906.2:c.2529C>A