Allele Registry

Canonical Allele Identifier: PA106053

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000015124

RCV002513057

ClinVar Variation:

14077

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Thr1155Ile	CA257093 NM_002473.6:c.3464C>T