Canonical Allele Identifier: PA2827975987
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1097Ala
CA008333
NM_001354899.2:c.3290T>C