Canonical Allele Identifier: PA2827943620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile1311Ser
CA10578361
NM_001354895.2:c.3932T>G