Canonical Allele Identifier: PA916041531
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2570Cys
CA16037960
NM_001354896.2:c.7708A>T