Allele Registry

Canonical Allele Identifier: PA645294962

Gene: MYH9 HGNC NCBI

ClinVar Allele:

338030

ClinVar RCV:

RCV000343175

RCV000392449

RCV003727702

ClinVar Variation:

341492

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Thr1906Met	CA10208952 NM_002473.6:c.5717C>T