Canonical Allele Identifier: PA2827950758
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1063950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1029Val
CA16027966
NM_001354896.2:c.3086C>T