Canonical Allele Identifier: PA2827999210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp2604Gly
CA16038681
NM_001354901.2:c.7811A>G