Allele Registry

Canonical Allele Identifier: PA105992

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000032224

RCV000790359

RCV002513293

ClinVar Variation:

38966

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asp1424Tyr	CA343280 NM_002473.6:c.4270G>T