Canonical Allele Identifier: PA2827943623
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly1312Ala
CA008783
NM_001354895.2:c.3935G>C