Canonical Allele Identifier: PA916042288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg978Gly
CA008168
NM_001354902.2:c.2932A>G