Canonical Allele Identifier: PA2828004202
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2460Leu
CA16037955
NM_001354902.2:c.7379A>T