Canonical Allele Identifier: PA2828027226
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2035Gly
CA046510
NM_001354906.2:c.6103A>G