Canonical Allele Identifier: PA2825025001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2635Ala
CA10622269
NM_000038.6:c.7903A>G