Canonical Allele Identifier: PA2825019084
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1160Ala
CA035507
NM_000038.6:c.3478A>G