Allele Registry

Canonical Allele Identifier: PA306581

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000182523

RCV000778043

RCV001088950

ClinVar Variation:

201079

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Asp1579Asn	CA306580 NM_002474.3:c.4735G>A