Canonical Allele Identifier: PA2827968337
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Cys1553Gly
CA009712
NM_001354898.2:c.4657T>G