Canonical Allele Identifier: PA2827986292
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1452Met
CA009574
NM_001354900.2:c.4355C>T