Canonical Allele Identifier: PA114122
Gene: VWF HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.2:p.Trp1313Cys
CA114121
NM_000552.4:c.3939G>C
CA383506117
NM_000552.4:c.3939G>T