Canonical Allele Identifier: PA2828014084
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2639Pro
CA16039553
NM_001354905.2:c.7915T>C