Canonical Allele Identifier: PA2573063261
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 256669
ClinVar RCV Id: RCV000254215 RCV000283100 RCV002264675
ClinVar Variation Id: 619934
ClinVar RCV Id: RCV000760120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Pro1162Leu
CA6402756
NM_000552.5:c.3485C>T
CA658683073
NM_000552.5:c.3485_3486delinsTG