Canonical Allele Identifier: PA658659720
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1160Ala
CA035507
NM_001127510.3:c.3478A>G