Allele Registry

Canonical Allele Identifier: PA105975

Gene: MYH9 HGNC NCBI

ClinVar Allele:

29115

ClinVar RCV:

RCV000032223

ClinVar Variation:

14076

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asp1424His	CA257091 NM_002473.6:c.4270G>C