Canonical Allele Identifier: PA2573063115
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 256677
ClinVar RCV Id: RCV000246724 RCV000382333 RCV002272194 RCV002244012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly131Ser
CA6403810
NM_000552.5:c.391G>A