Canonical Allele Identifier: PA916039684
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg658Trp
CA16025509
NM_001354896.2:c.1972C>T