Canonical Allele Identifier: PA2828021964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1392Met
CA009574
NM_001354903.2:c.4175C>T