Canonical Allele Identifier: PA272854
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1640Trp
CA009806
NM_001127510.3:c.4918C>T