Allele Registry

Canonical Allele Identifier: PA105945

Gene: MYH9 HGNC NCBI

ClinVar Allele:

29118

ClinVar RCV:

RCV000015130

RCV000032218

RCV001659697

ClinVar Variation:

14079

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg705His	CA257097 NM_002473.6:c.2114G>A