Allele Registry

Canonical Allele Identifier: PA105917

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000032221

ClinVar Variation:

38965

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1165Leu	CA343278 NM_002473.6:c.3494G>T