Allele Registry

Canonical Allele Identifier: PA273198

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000151326

RCV001850061

RCV002478429

ClinVar Variation:

164432

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Val1516Leu	CA273196 NM_002473.6:c.4546G>T CA411379605 NM_002473.6:c.4546G>C