Canonical Allele Identifier: PA165687
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Phe2620Ile
CA014111
NM_001127510.3:c.7858T>A