Canonical Allele Identifier: PA2573063358
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100346
ClinVar RCV Id: RCV000086751 RCV002227446 RCV002498470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ile1425Phe
CA228573
NM_000552.5:c.4273A>T