Canonical Allele Identifier: PA2828018007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser598Phe
CA348575
NM_001354906.2:c.1793C>T