Canonical Allele Identifier: PA2827971383
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 575302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu2482Phe
CA16037679
NM_001354898.2:c.7444C>T