Canonical Allele Identifier: PA2825641321
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1506Val
CA16031338
NM_001127511.3:c.4516A>G