Canonical Allele Identifier: PA2827950949
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1087Gly
CA008168
NM_001354896.2:c.3259A>G