Allele Registry

Canonical Allele Identifier: PA105952

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000015122

RCV000790350

ClinVar Variation:

14075

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asn93Lys	CA257089 NM_002473.6:c.279C>G CA411549137 NM_002473.6:c.279C>A