Allele Registry

Canonical Allele Identifier: PA645294947

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000285049

RCV000408217

RCV000997915

ClinVar Variation:

341507

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1342Gln	CA10209485 NM_002473.6:c.4025G>A