Canonical Allele Identifier: PA2827971525
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2527Cys
CA16037960
NM_001354898.2:c.7579A>T