Canonical Allele Identifier: PA2828027315
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2047Phe
CA16036569
NM_001354906.2:c.6140C>T