Canonical Allele Identifier: PA916039984
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu940Phe
CA033363
NM_001354896.2:c.2818C>T