Canonical Allele Identifier: PA2828004093
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 657079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu2397Arg
CA16037570
NM_001354902.2:c.7190T>G