Canonical Allele Identifier: PA2827942757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1058Gly
CA008117
NM_001354895.2:c.3173A>G