Canonical Allele Identifier: PA2828016633
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg539Trp
CA16025509
NM_001354903.2:c.1615C>T