Canonical Allele Identifier: PA2827943121
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr1160Ala
CA035507
NM_001354895.2:c.3478A>G