Canonical Allele Identifier: PA2828019078
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg757Trp
CA008046
NM_001354906.2:c.2269A>T