Canonical Allele Identifier: PA228666
Gene: VWF HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.2:p.Gly1609Arg
CA228665
NM_000552.4:c.4825G>A
CA383499042
NM_000552.4:c.4825G>C