Canonical Allele Identifier: PA2828028732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu2256Phe
CA10578447
NM_001354906.2:c.6766C>T