Canonical Allele Identifier: PA2828001613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1042Val
CA16028781
NM_001354902.2:c.3125A>T