Canonical Allele Identifier: PA2828020739
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile1028Ser
CA10578361
NM_001354906.2:c.3083T>G