Canonical Allele Identifier: PA2827951193
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1164Cys
CA035367
NM_001354896.2:c.3490C>T