Canonical Allele Identifier: PA916071899
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 262426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620596.2:p.Gln456His
CA10587032
NM_139027.6:c.1368G>T
CA375391658
NM_139027.6:c.1368G>C