Canonical Allele Identifier: PA3079268613
Gene: VWF HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Thr1381Ser
CA383504417
NM_000552.5:c.4142C>G
CA383504420
NM_000552.5:c.4141A>T