Canonical Allele Identifier: PA916042268
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181783
ClinVar Variation Id: 919990
ClinVar RCV Id: RCV001178470
ClinVar Variation Id: 3231860
ClinVar RCV Id: RCV004518575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser316Arg
CA015653
NM_001354902.2:c.948T>G
CA16023314
NM_001354902.2:c.946A>C
CA16023320
NM_001354902.2:c.948T>A