Canonical Allele Identifier: PA2828001364
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1063950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala920Val
CA16027966
NM_001354902.2:c.2759C>T