Canonical Allele Identifier: PA2828028669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 575302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu2406Phe
CA16037679
NM_001354903.2:c.7216C>T