Allele Registry

Canonical Allele Identifier: PA645295089

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000251625

RCV003629099

ClinVar Variation:

14134

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Arg1275Leu	CA257130 NM_002474.3:c.3824G>T