Canonical Allele Identifier: PA2825024720
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2567Ser
CA16038056
NM_000038.6:c.7699A>T
CA16038058
NM_000038.6:c.7700C>G