Canonical Allele Identifier: PA2825021351
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 964536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1700Pro
CA16032478
NM_000038.6:c.5098G>C