Canonical Allele Identifier: PA2573063259
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100264
ClinVar RCV Id: RCV000086659 RCV000851957 RCV001787053 RCV002264645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Thr1156Met
CA228414
NM_000552.5:c.3467C>T