Allele Registry

Canonical Allele Identifier: PA645294958

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000287421

RCV000323686

ClinVar Variation:

341496

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1658Cys	CA10209219 NM_002473.6:c.4972C>T