Canonical Allele Identifier: PA658688657
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2243Ala
CA045904
NM_001127510.3:c.6727A>G