Canonical Allele Identifier: PA2828018339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu821Phe
CA033363
NM_001354903.2:c.2461C>T