Canonical Allele Identifier: PA2828001220
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu831Phe
CA033363
NM_001354902.2:c.2491C>T