Canonical Allele Identifier: PA2828000521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu457Val
CA16024895
NM_001354902.2:c.1369T>G