Canonical Allele Identifier: PA2828005696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1160Glu
CA037191
NM_001354905.2:c.3479T>A