Canonical Allele Identifier: PA2825641715
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2726917
ClinVar RCV Id: RCV003539016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser1634Ala
CA16032181
NM_001127511.3:c.4900T>G