Canonical Allele Identifier: PA2827975297
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Leu894Phe
CA033363
NM_001354899.2:c.2680C>T