Allele Registry

Canonical Allele Identifier: PA105908

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000015121

RCV000790357

RCV001092004

RCV001270614

RCV001542710

ClinVar Variation:

14074

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1165Cys	CA257087 NM_002473.6:c.3493C>T