Canonical Allele Identifier: PA2828029160
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 654022
ClinVar RCV Id: RCV003653372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Glu2320Asp
CA16038295
NM_001354906.2:c.6960A>C
CA16038296
NM_001354906.2:c.6960A>T