Canonical Allele Identifier: PA2827943508
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1275Thr
CA008695
NM_001354895.2:c.3824G>C