Canonical Allele Identifier: PA2828004729
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2848991
ClinVar RCV Id: RCV003744530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser26Gly
CA360611870
NM_001354902.2:c.76A>G