Canonical Allele Identifier: PA2827977925
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 919682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1680Glu
CA16032527
NM_001354899.2:c.5039T>A