Canonical Allele Identifier: PA2825637640
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1764696
ClinVar RCV Id: RCV002373690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser275Arg
CA16023234
NM_001127511.3:c.823A>C
CA16023240
NM_001127511.3:c.825T>A
CA16023241
NM_001127511.3:c.825T>G