Canonical Allele Identifier: PA2828053348
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr402Met
CA005437
NM_001354905.2:c.1205C>T