Canonical Allele Identifier: PA2828023822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1654Val
CA041104
NM_001354903.2:c.4961C>T