Canonical Allele Identifier: PA2827954003
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2579Ile
CA16038011
NM_001354896.2:c.7735G>A