Canonical Allele Identifier: PA2827980554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 575302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Leu2479Phe
CA16037679
NM_001354899.2:c.7435C>T