Canonical Allele Identifier: PA916040447
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1658Trp
CA009806
NM_001354896.2:c.4972C>T