Canonical Allele Identifier: PA2828051309
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr181Arg
CA047191
NM_001354905.2:c.542C>G