Canonical Allele Identifier: PA2827982282
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr181Arg
CA047191
NM_001354900.2:c.542C>G