Allele Registry

Canonical Allele Identifier: PA645294959

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000454246

ClinVar Variation:

402285

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Ser1713Gly	CA10209162 NM_002473.6:c.5137A>G