Allele Registry

Canonical Allele Identifier: PA2826068371

Gene: MYD88 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

45735

ClinVar RCV:

RCV000030709

RCV000425047

RCV000431830

RCV000442854

RCV000443819

RCV000646119

RCV003315524

ClinVar Variation:

37055

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166039.2:p.Leu207Pro	CA130043 NM_001172568.2:c.620T>C