Canonical Allele Identifier: PA2573063421
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 439343
ClinVar RCV Id: RCV000508422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1625Leu
CA383498796
NM_000552.5:c.4873G>T
CA383498798
NM_000552.5:c.4873G>C