Canonical Allele Identifier: PA658691755
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr240Arg
CA047191
NM_001127510.3:c.719C>G