Canonical Allele Identifier: PA2825021280
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 850938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Phe1684Ser
CA16032377
NM_000038.6:c.5051T>C