Canonical Allele Identifier: PA2573063354
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 439338
ClinVar RCV Id: RCV000506329 RCV001563671 RCV003447537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ile1416Thr
CA383503536
NM_000552.5:c.4247T>C