Allele Registry

Canonical Allele Identifier: PA645393281

Gene: MYH9 HGNC NCBI

ClinVar Allele:

29124

612065

ClinVar RCV:

RCV000015141

RCV000790342

ClinVar Variation:

14085

623098

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Gln1068_Leu1074dup