Canonical Allele Identifier: PA2827978100
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1729Cys
CA16032852
NM_001354899.2:c.5186C>G