Canonical Allele Identifier: PA1139765718
Gene: EXT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954538
ClinVar RCV Id: RCV001227008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997005.1:p.Met87Ile
CA5954851
NM_207122.2:c.261G>A
CA380179962
NM_207122.2:c.261G>C
CA380179963
NM_207122.2:c.261G>T