Allele Registry

Canonical Allele Identifier: PA2825440741

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV000002282

ClinVar Variation:

2198

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070654.1:p.Arg734Ser	CA252135 NM_001077186.2:c.2200C>A