Canonical Allele Identifier: PA2828003783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala2195Val
CA012589
NM_001354902.2:c.6584C>T