Canonical Allele Identifier: PA2828000288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln354Glu
CA10578313
NM_001354902.2:c.1060C>G