Canonical Allele Identifier: PA2825644592
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827236
ClinVar RCV Id: RCV001026779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu2564Gly
CA16038152
NM_001127511.3:c.7691A>G