Allele Registry

Canonical Allele Identifier: PA177071

Gene: MYH9 HGNC NCBI

ClinVar Allele:

176256

ClinVar RCV:

RCV000151322

RCV000416222

RCV001150618

RCV001150619

RCV001375382

ClinVar Variation:

164421

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Lys1676Glu	CA177069 NM_002473.6:c.5026A>G