Canonical Allele Identifier: PA2827981622
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2803Leu
CA050906
NM_001354899.2:c.8408C>T