Canonical Allele Identifier: PA2828031190
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser105Gly
CA008731
NM_001354904.2:c.313A>G