Canonical Allele Identifier: PA645384632
Gene: ADAMTS13 HGNC NCBI

Linked Data

ClinVar Variation Id: 262426
ClinVar RCV Id: RCV000246702 RCV000375633 RCV000972467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620594.1:p.Gln456His
CA10587032
NM_139025.5:c.1368G>T
CA375391658
NM_139025.5:c.1368G>C