Canonical Allele Identifier: PA2828023654
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys1488Arg
CA16032947
NM_001354906.2:c.4463A>G