Canonical Allele Identifier: PA2830271506
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2139046
ClinVar RCV Id: RCV003066493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620594.1:p.Pro952Ser
CA200939153
NM_139025.5:c.2854C>T