Canonical Allele Identifier: PA2828004725
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2971260
ClinVar RCV Id: RCV003827442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Trp25Arg
CA360611855
NM_001354902.2:c.73T>A
CA360611856
NM_001354902.2:c.73T>C