Allele Registry

Canonical Allele Identifier: PA2580275892

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV002266358

ClinVar Variation:

1696214

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Val1516Met	CA411379606 NM_002473.6:c.4546G>A