Allele Registry

Canonical Allele Identifier: PA645295067

Gene: MYH11 HGNC NCBI

ClinVar Variation Id: 263472

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Thr667Met	CA7922457 NM_002474.3:c.2000C>T