Canonical Allele Identifier: PA645400133
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys1543Glu
CA10578378
NM_001127510.3:c.4627A>G