Canonical Allele Identifier: PA916040082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1329Ser
CA10578361
NM_001354896.2:c.3986T>G