Allele Registry

Canonical Allele Identifier: PA915995126

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000851788

RCV001855730

ClinVar Variation:

627067

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asp1447Gly	CA411381860 NM_002473.6:c.4340A>G