Canonical Allele Identifier: PA2825015899
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr621Ile
CA16025395
NM_000038.6:c.1862C>T