Canonical Allele Identifier: PA2825021394
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 649664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1709Ile
CA16032535
NM_000038.6:c.5126C>T