Canonical Allele Identifier: PA2828042778
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala1629Val
CA041104
NM_001354904.2:c.4886C>T