Canonical Allele Identifier: PA2825015072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp459Gly
CA16024318
NM_000038.6:c.1376A>G