Canonical Allele Identifier: PA2828004261
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2500Leu
CA16038216
NM_001354902.2:c.7499A>T