Canonical Allele Identifier: PA2825644878
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2656Pro
CA16038751
NM_001127511.3:c.7966T>C