Canonical Allele Identifier: PA2827983931
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser746Gly
CA031761
NM_001354900.2:c.2236A>G