Canonical Allele Identifier: PA16039833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg414Ser
CA10578311
NM_000038.6:c.1240C>A