Canonical Allele Identifier: PA2825014053
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser290Arg
CA16023216
NM_000038.6:c.868A>C
CA16023221
NM_000038.6:c.870T>A
CA16023222
NM_000038.6:c.870T>G