Canonical Allele Identifier: PA916041430
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2486Pro
CA013665
NM_001354896.2:c.7456T>C