Canonical Allele Identifier: PA105023
Gene: ADAMTSL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 524194
ClinVar RCV Id: RCV000627668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138792.1:p.Ala165Thr
CA5312634
NM_001145320.2:c.493G>A