Canonical Allele Identifier: PA916042198
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr250Arg
CA047191
NM_001354902.2:c.749C>G