Canonical Allele Identifier: PA658660974
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2799Pro
CA16039553
NM_001127510.3:c.8395T>C