Canonical Allele Identifier: PA2825024962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2627Phe
CA049365
NM_000038.6:c.7880C>T