Allele Registry

Canonical Allele Identifier: PA2825440739

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV001765235

ClinVar Variation:

1305060

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070654.1:p.Arg734Cys	CA406944924 NM_001077186.2:c.2200C>T