Canonical Allele Identifier: PA2827967450
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1287Ala
CA008783
NM_001354898.2:c.3860G>C