Allele Registry

Canonical Allele Identifier: PA658816318

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000626824

RCV000852126

ClinVar Variation:

523453

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asp1424Gly	CA323590385 NM_002473.6:c.4271A>G