Canonical Allele Identifier: PA916042681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr935Met
CA008612
NM_001354906.2:c.2804C>T