Canonical Allele Identifier: PA2825013577
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr240Arg
CA047191
NM_000038.6:c.719C>G