Allele Registry

Canonical Allele Identifier: PA177068

Gene: MYH9 HGNC NCBI

ClinVar Allele:

176376

ClinVar RCV:

RCV000151321

RCV001575204

ClinVar Variation:

164417

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1730Cys	CA177066 NM_002473.6:c.5188C>T