Canonical Allele Identifier: PA2828019689
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp850Val
CA16028781
NM_001354906.2:c.2549A>T