Allele Registry

Canonical Allele Identifier: PA106031

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000151335

RCV000268989

RCV000363597

RCV000767070

RCV000990431

ClinVar Variation:

164442

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Ser1114Pro	CA177103 NM_002473.6:c.3340T>C