Canonical Allele Identifier: PA2828028879
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927393
ClinVar RCV Id: RCV001190628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Leu2275Val
CA048920
NM_001354906.2:c.6823C>G