Canonical Allele Identifier: PA916042446
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val999Ala
CA008333
NM_001354904.2:c.2996T>C