Canonical Allele Identifier: PA215543
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2568Ile
CA014009
NM_001127511.3:c.7703G>T