Canonical Allele Identifier: PA2827989799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2516Cys
CA16037994
NM_001354900.2:c.7547C>G