Allele Registry

Canonical Allele Identifier: PA092491

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV000002282

ClinVar Variation:

2198

HGVS (amino-acid)	Matching Registered Transcripts
NP_079005.3:p.Arg726Ser	CA252135 NM_024729.4:c.2176C>A