Allele Registry

Canonical Allele Identifier: PA658816250

Gene: MYH9 HGNC NCBI

ClinVar Allele:

497763

ClinVar RCV:

RCV000613271

RCV001143858

RCV001143859

RCV001573754

RCV002531129

ClinVar Variation:

504627

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Tyr11Cys	CA10210738 NM_002473.6:c.32A>G