Canonical Allele Identifier: PA2828018885
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp733Val
CA16028005
NM_001354906.2:c.2198A>T