Canonical Allele Identifier: PA2827994649
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1216Thr
CA008695
NM_001354901.2:c.3647G>C