Canonical Allele Identifier: PA2827990587
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2758Pro
CA16039553
NM_001354900.2:c.8272T>C