Allele Registry

Canonical Allele Identifier: PA645395494

Gene: MYH14 HGNC NCBI

ClinVar RCV:

RCV000214901

RCV001133104

RCV001505041

RCV003929907

ClinVar Variation:

228871

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139281.1:p.Arg640Gln	CA9592748 NM_001145809.2:c.1919G>A