Canonical Allele Identifier: PA2827968590
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1633Thr
CA16032217
NM_001354898.2:c.4898G>C