Canonical Allele Identifier: PA156791
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2268Val
CA012589
NM_001127511.3:c.6803C>T