Canonical Allele Identifier: PA2825640203
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1146Val
CA16028993
NM_001127511.3:c.3436A>G