Canonical Allele Identifier: PA2827989827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2526Ser
CA16038056
NM_001354900.2:c.7576A>T
CA16038058
NM_001354900.2:c.7577C>G