Canonical Allele Identifier: PA2828023395
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1596Ala
CA10578392
NM_001354903.2:c.4786A>G