Canonical Allele Identifier: PA2828032148
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser265Arg
CA16023216
NM_001354904.2:c.793A>C
CA16023221
NM_001354904.2:c.795T>A
CA16023222
NM_001354904.2:c.795T>G