Canonical Allele Identifier: PA2827971600
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 960729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2550Pro
CA16038103
NM_001354898.2:c.7648T>C