Canonical Allele Identifier: PA916040511
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1715Ala
CA10578392
NM_001354896.2:c.5143A>G