Canonical Allele Identifier: PA297880
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile2206Val
CA012361
NM_001127511.3:c.6616A>G