Canonical Allele Identifier: PA286611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg1571His
CA009743
NM_001127511.3:c.4712G>A