Allele Registry

Canonical Allele Identifier: PA645294934

Gene: MYH9 HGNC NCBI

ClinVar RCV:

RCV000262620

RCV000359728

RCV001753803

RCV002523222

ClinVar Variation:

341519

HGVS (amino-acid)	Matching Registered Transcripts
NP_002464.1:p.Asn866Lys	CA10209927 NM_002473.6:c.2598C>G CA411394445 NM_002473.6:c.2598C>A