Canonical Allele Identifier: PA2828040509
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1367Met
CA009574
NM_001354904.2:c.4100C>T