Allele Registry

Canonical Allele Identifier: PA2829397952

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000414859

ClinVar Variation:

374162

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Asp1454His	CA16043500 NM_002474.3:c.4360G>C