Canonical Allele Identifier: PA2573063311
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 300
ClinVar RCV Id: RCV000000327 RCV000086716 RCV003447468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Gly1324Ser
CA114147
NM_000552.5:c.3970G>A