Canonical Allele Identifier: PA916041810
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2817Pro
CA16039553
NM_001354896.2:c.8449T>C