Canonical Allele Identifier: PA2828024657
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1778Ser
CA010547
NM_001354903.2:c.5332G>T