Canonical Allele Identifier: PA2828029204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760789
ClinVar RCV Id: RCV002412102
ClinVar Variation Id: 2106397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly2327Arg
CA16038337
NM_001354906.2:c.6979G>A
CA16038338
NM_001354906.2:c.6979G>C