Canonical Allele Identifier: PA2827994056
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg1046Trp
CA034994
NM_001354901.2:c.3136C>T