Canonical Allele Identifier: PA2825013408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala219Thr
CA16022765
NM_000038.6:c.655G>A