Canonical Allele Identifier: PA2827951242
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1178Ala
CA035507
NM_001354896.2:c.3532A>G