Canonical Allele Identifier: PA2825018211
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser1028Ile
CA16028086
NM_000038.6:c.3083G>T