Allele Registry

Canonical Allele Identifier: PA2829996641

Gene: MYH11 HGNC NCBI

ClinVar Variation Id: 465724

HGVS (amino-acid)	Matching Registered Transcripts
NP_074035.1:p.Leu1127Val	CA394861996 NM_022844.3:c.3379C>G