Canonical Allele Identifier: PA2827994128
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val1066Ala
CA008333
NM_001354901.2:c.3197T>C