Canonical Allele Identifier: PA2828049947
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2673Pro
CA16039553
NM_001354904.2:c.8017T>C