Canonical Allele Identifier: PA2827989717
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1321396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2492Cys
CA16037837
NM_001354900.2:c.7475C>G