Canonical Allele Identifier: PA2827991900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg355Ser
CA10578311
NM_001354901.2:c.1063C>A