Canonical Allele Identifier: PA2827989798
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2516Phe
CA16037995
NM_001354900.2:c.7547C>T