Allele Registry

Canonical Allele Identifier: PA177101

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000151333

RCV000291994

RCV000386272

RCV000724779

ClinVar Variation:

164439

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asp1409Asn	CA177099 NM_002473.6:c.4225G>A