Allele Registry

Canonical Allele Identifier: PA134548

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000032225

RCV000037563

RCV000368736

RCV000402895

RCV002054532

RCV002504851

ClinVar Variation:

38967

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Ile1626Val	CA134546 NM_002473.6:c.4876A>G