Allele Registry

Canonical Allele Identifier: PA645294927

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000424167

RCV000790339

ClinVar Variation:

377017

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Phe41Ser	CA16603232 NM_002473.6:c.122T>C