Canonical Allele Identifier: PA2828000755
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile585Val
CA030596
NM_001354902.2:c.1753A>G