Canonical Allele Identifier: PA2825021318
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1692Ala
CA16032425
NM_000038.6:c.5074A>G