Canonical Allele Identifier: PA2827966351
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile958Thr
CA007931
NM_001354898.2:c.2873T>C