Canonical Allele Identifier: PA2828002739
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg1604Gly
CA040621
NM_001354902.2:c.4810A>G