Canonical Allele Identifier: PA2825025330
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537538
ClinVar RCV Id: RCV003538504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2715Ala
CA16039014
NM_000038.6:c.8143A>G