Allele Registry

Canonical Allele Identifier: PA257129

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV001938595

ClinVar Variation:

1417736

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Leu1264Pro	CA257128 NM_001040113.2:c.3791T>C