Canonical Allele Identifier: PA2827989647
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 664699
ClinVar Variation Id: 1759394
ClinVar RCV Id: RCV002393894
ClinVar Variation Id: 3231329
ClinVar RCV Id: RCV004525400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2471Arg
CA16037706
NM_001354900.2:c.7411A>C
CA16037712
NM_001354900.2:c.7413T>A
CA16037713
NM_001354900.2:c.7413T>G