Canonical Allele Identifier: PA2825015998
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser643Phe
CA16025529
NM_000038.6:c.1928C>T