Canonical Allele Identifier: PA2828019669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg1013Leu
CA16028658
NM_001354903.2:c.3038G>T