Canonical Allele Identifier: PA916041677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2704Ala
CA049793
NM_001354896.2:c.8111T>C