Canonical Allele Identifier: PA2828023199
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1569Val
CA009818
NM_001354903.2:c.4706C>T