Canonical Allele Identifier: PA2828000705
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu565Val
CA030483
NM_001354902.2:c.1693C>G