Canonical Allele Identifier: PA2825636392
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1692Ala
CA16032425
NM_001127510.3:c.5074A>G