Canonical Allele Identifier: PA2827987566
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1838Ser
CA010547
NM_001354900.2:c.5512G>T