Canonical Allele Identifier: PA2825633413
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1501504
ClinVar RCV Id: RCV003773324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1676Ser
CA16032329
NM_001127510.3:c.5028A>C
CA16032330
NM_001127510.3:c.5028A>T