Canonical Allele Identifier: PA2828029055
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2466Ser
CA16038056
NM_001354903.2:c.7396A>T
CA16038058
NM_001354903.2:c.7397C>G