Allele Registry

Canonical Allele Identifier: PA306582

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000182523

RCV000778043

RCV001088950

ClinVar Variation:

201079

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Asp1586Asn	CA306580 NM_001040113.2:c.4756G>A