Canonical Allele Identifier: PA2828020716
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile1210Ser
CA10578361
NM_001354903.2:c.3629T>G