Allele Registry

Canonical Allele Identifier: PA134536

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000037559

RCV000346916

RCV000382897

RCV000990430

RCV000992411

ClinVar Variation:

44562

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Arg1400Trp	CA134534 NM_002473.6:c.4198C>T