Canonical Allele Identifier: PA2827996020
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg1636Gly
CA040621
NM_001354901.2:c.4906A>G