Canonical Allele Identifier: PA2827981272
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Leu2694Pro
CA050043
NM_001354899.2:c.8081T>C