Canonical Allele Identifier: PA167748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg1022Trp
CA008046
NM_001127511.3:c.3064A>T