Canonical Allele Identifier: PA2828046864
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2226Gly
CA16036702
NM_001354904.2:c.6676A>G