Canonical Allele Identifier: PA2827970969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu2359Ile
CA047103
NM_001354898.2:c.7075T>A