Canonical Allele Identifier: PA2825639024
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser769Gly
CA031761
NM_001127511.3:c.2305A>G