Canonical Allele Identifier: PA2825645254
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2781Pro
CA16039553
NM_001127511.3:c.8341T>C