Canonical Allele Identifier: PA2827980913
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu2591Ala
CA10578452
NM_001354899.2:c.7772A>C