Canonical Allele Identifier: PA2828028554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp2389Val
CA048153
NM_001354903.2:c.7166A>T