Allele Registry

Canonical Allele Identifier: PA645294957

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000283777

RCV000378271

RCV002524453

ClinVar Variation:

341497

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1652His	CA10209226 NM_002473.6:c.4955G>A