Allele Registry

Canonical Allele Identifier: PA2829182841

Gene: EXT2 HGNC NCBI

ClinVar Variation Id: 954538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001376557.1:p.Met87Ile	CA5954851 NM_001389628.1:c.261G>A CA380179962 NM_001389628.1:c.261G>C CA380179963 NM_001389628.1:c.261G>T