Canonical Allele Identifier: PA2827990535
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala2737Ser
CA014561
NM_001354900.2:c.8209G>T