Canonical Allele Identifier: PA2827940195
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr240Arg
CA047191
NM_001354895.2:c.719C>G