Canonical Allele Identifier: PA1139733715
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala44Thr
CA053928
NM_001354902.2:c.130G>A