Canonical Allele Identifier: PA2827998434
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2370Cys
CA16037199
NM_001354901.2:c.7109C>G