Canonical Allele Identifier: PA645398852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg414Ser
CA10578311
NM_001127510.3:c.1240C>A