Canonical Allele Identifier: PA2828027479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2069Gly
CA16036702
NM_001354906.2:c.6205A>G