Canonical Allele Identifier: PA2828001573
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His1028Leu
CA16028686
NM_001354902.2:c.3083A>T