Canonical Allele Identifier: PA2827971020
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2373Phe
CA012909
NM_001354898.2:c.7118C>T