Allele Registry

Canonical Allele Identifier: PA645294951

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000216020

RCV001150836

RCV001150837

RCV001555721

ClinVar Variation:

228928

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Thr1416Met	CA10209422 NM_002473.6:c.4247C>T