Canonical Allele Identifier: PA2828027666
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2251Gly
CA16036702
NM_001354903.2:c.6751A>G