Canonical Allele Identifier: PA2825639408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232412
ClinVar Variation Id: 663857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly889Arg
CA033124
NM_001127511.3:c.2665G>A
CA033134
NM_001127511.3:c.2665G>C