Allele Registry

Canonical Allele Identifier: PA2826068457

Gene: MYD88 HGNC NCBI

ClinVar RCV:

RCV000030709

RCV000425047

RCV000431830

RCV000442854

RCV000443819

RCV000646119

RCV003315524

ClinVar Variation:

37055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166040.2:p.Asp191_Ter192insArgSerProSerSerThrArgGln	CA130043 NM_001172569.3:c.574T>C CA352134298 NM_001172569.3:c.574T>A