Allele Registry

Canonical Allele Identifier: PA915994917

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000851737

ClinVar Variation:

627035

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg702Ser	CA411397435 NM_002473.6:c.2104C>A