Canonical Allele Identifier: PA2825022193
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1921Ser
CA16033936
NM_000038.6:c.5761G>A